ClinVar Miner

Submissions for variant NM_003331.5(TYK2):c.660C>G (p.Arg220=)

gnomAD frequency: 0.00001  dbSNP: rs772782888
Minimum review status: Collection method:
Minimum conflict level:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001486777 SCV001691253 likely benign Immunodeficiency 35 2024-10-24 criteria provided, single submitter clinical testing

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